Recall database

System, Gastrointestinal Motility (Electrical) recalls

Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.

Showing 1–2 of 2 recalls

Class IIOngoingZ-2950-2026

Covidien, LLC recalls EndoFLIP System that includes: ENDOFLIP 1 SYSTEM EF-100 05391530810050 1088452180930…

The system's 24-hour usage limit results in catheters incorrectly flagged as expired, making them unavailable for clinical procedures.

Gastrointestinal Motility (Electrical) System
Under Investigation by firm

Covidien, LLCCAAug 26, 2026

Class IIOngoingZ-2669-2026

Laborie Medical Technologies Corp recalls Solar GI System (Water Perfusion)

Under extended clinical use conditions (e.g., long duration studies), moisture generated within the pneumatic circuit may accumulate inside the system's internal tubing or at the hydrophobic filter and waterproof pressur…

Gastrointestinal Motility (Electrical) System
Device Design

Laborie Medical Techno…NHJul 8, 2026